Literature DB >> 20875654

Hastifolins A-G, antifeedant neo-clerodane diterpenoids from Scutellaria hastifolia.

Rosa Angela Raccuglia1, Gabriella Bellone, Kristina Loziene, Franco Piozzi, Sergio Rosselli, Antonella Maggio, Maurizio Bruno, Monique S J Simmonds.   

Abstract

From the aerial parts of Scutellaria hastifolia, family Lamiaceae (Labiatae), seven neo-clerodane diterpenoids (hastifolins A-G) were isolated. The products are similar to the known scuteparvin and are characterized by being trans-cinnamoyl derivatives. Structures and stereochemistry were determined by intensive NMR investigation. Six of the products form three pairs of epimers at C-13. Hastifolins A-C showed significant antifeedant activity.
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20875654     DOI: 10.1016/j.phytochem.2010.08.021

Source DB:  PubMed          Journal:  Phytochemistry        ISSN: 0031-9422            Impact factor:   4.072


  3 in total

1.  Acylated neo-clerodane type diterpenoids from the aerial parts of Scutellaria coleifolia Levl. (Lamiaceae).

Authors:  Shin-Ichiro Kurimoto; Jian-Xin Pu; Han-Dong Sun; Hirofumi Shibata; Yoshihisa Takaishi; Yoshiki Kashiwada
Journal:  J Nat Med       Date:  2016-01-29       Impact factor: 2.343

Review 2.  Clerodane diterpenes: sources, structures, and biological activities.

Authors:  Rongtao Li; Susan L Morris-Natschke; Kuo-Hsiung Lee
Journal:  Nat Prod Rep       Date:  2016-07-18       Impact factor: 13.423

3.  Rhodium(i)-catalyzed asymmetric [4 + 2] cycloaddition reactions of 2-alkylenecyclobutanols with cyclic enones through C-C bond cleavage: efficient access to trans-bicyclic compounds.

Authors:  Xinxin Zheng; Rui Guo; Guozhu Zhang; Dayong Zhang
Journal:  Chem Sci       Date:  2018-01-08       Impact factor: 9.825

  3 in total

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